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临床试验/NCT06146049
NCT06146049尚未招募不适用

Examination of Participation Trends and Engagement Patterns of Participants in Post Traumatic Stress Disorder Clinical Trials

Power Life Sciences Inc.1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2024年12月最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
500
试验地点
1
主要终点
Number of post traumatic stress disorder study participants who remain in clinical study until completion.

研究概览

简要总结

Participation in post traumatic stress disorder observational study serves as a crucial contribution to advancing medical knowledge and refining the care provided to individuals facing similar health challenges.

The primary objective centers on a meticulous examination of trial completion rates and voluntary withdrawals within this distinct patient population.

研究设计

研究类型
Observational
观察模型
Case Crossover
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of post traumatic stress disorder
  • No prior treatment for post traumatic stress disorder
  • Willing and able to provide informed consent.

排除标准

  • Enrolled in another research study
  • Psychiatric or behavioral illness
  • Inability to provide written informed consent

结局指标

主要结局

Number of post traumatic stress disorder study participants who remain in clinical study until completion.

时间窗: 12 months

Rate of patients who decide to enroll in a post traumatic stress disorder clinical research.

时间窗: 3 months

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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